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3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester

Base Information Edit
  • Chemical Name:3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester
  • CAS No.:1027968-84-8
  • Molecular Formula:C36H37ClO7
  • Molecular Weight:617.139
  • Hs Code.:
  • Mol file:1027968-84-8.mol
3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester

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Chemical Property of 3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester Edit
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Technology Process of 3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester

There total 9 articles about 3-(3-Chlorocarbonyl-4,6-dimethoxy-2,5-dimethyl-benzyl)-4,6-dimethoxy-2,5-dimethyl-benzoic acid benzhydryl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With oxalyl dichloride; In dichloromethane; a) RT, 30 min, b) reflux, 30 min;
DOI:10.1021/jm960437a
Guidance literature:
Multi-step reaction with 5 steps
1: 100 percent / BF3*OEt2 / toluene / 0.25 h / Ambient temperature
2: 2.97 g / K2CO3 / acetone / Heating
3: 95 percent / aq. KOH / dimethylsulfoxide
4: ethyl acetate / Ambient temperature
5: oxalyl chloride / CH2Cl2 / a) RT, 30 min, b) reflux, 30 min
With potassium hydroxide; oxalyl dichloride; boron trifluoride diethyl etherate; potassium carbonate; In dichloromethane; dimethyl sulfoxide; ethyl acetate; acetone; toluene;
DOI:10.1021/jm960437a
Guidance literature:
Multi-step reaction with 8 steps
1: 6.8 g / K2CO3 / acetone / 2 h / Heating
2: 3.18 g / NaBH4 / propan-2-ol
3: 3.35 g / pyridine, (dimethylamino)pyridine / CH2Cl2 / 2 h / Ambient temperature
4: 100 percent / BF3*OEt2 / toluene / 0.25 h / Ambient temperature
5: 2.97 g / K2CO3 / acetone / Heating
6: 95 percent / aq. KOH / dimethylsulfoxide
7: ethyl acetate / Ambient temperature
8: oxalyl chloride / CH2Cl2 / a) RT, 30 min, b) reflux, 30 min
With pyridine; dmap; potassium hydroxide; sodium tetrahydroborate; oxalyl dichloride; boron trifluoride diethyl etherate; potassium carbonate; In dichloromethane; dimethyl sulfoxide; ethyl acetate; isopropyl alcohol; acetone; toluene;
DOI:10.1021/jm960437a
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